CHCHD2 and Parkinson's disease
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology
Reference4 articles.
1. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study;Funayama;Lancet Neurol,2015
2. Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations;Kachergus;Am J Hum Genet,2005
3. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study;Healy;Lancet Neurol,2008
4. A new gene for Parkinson's disease: should we care?;Singleton;Lancet Neurol,2015
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1. Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction;Neurology Genetics;2018-10
2. The delta‐opioid receptor and Parkinson’s disease;CNS Neuroscience & Therapeutics;2018-08-03
3. Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria;Neurobiology of Aging;2017-02
4. Genetic analysis of the CHCHD2 gene in Chinese patients with familial essential tremor;Neuroscience Letters;2016-11
5. Genetic analysis ofCHCHD2gene in Chinese Parkinson's disease;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2016-09-14
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